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FDA 510(k)

TOTAL BILIRUBIN REAGENT

K-Number: K881241 · 1988-05-27

Decision Date1988-05-27
Product CodeCIG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TOTAL BILIRUBIN REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Tech-Neal Scientific, Inc.. It received FDA 510(k) clearance on 1988-05-27 under 510(k) number K881241. The device is classified under product code CIG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOTAL BILIRUBIN REAGENT?

TOTAL BILIRUBIN REAGENT is a medical device that received FDA 510(k) clearance on 1988-05-27. The listed applicant is Tech-Neal Scientific, Inc.. The 510(k) number is K881241.

When did TOTAL BILIRUBIN REAGENT receive FDA 510(k) clearance?

TOTAL BILIRUBIN REAGENT received FDA 510(k) clearance on 1988-05-27, under 510(k) number K881241.

Who is the listed applicant for TOTAL BILIRUBIN REAGENT?

The FDA 510(k) record lists Tech-Neal Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOTAL BILIRUBIN REAGENT?

The FDA product code for TOTAL BILIRUBIN REAGENT is CIG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Tech-Neal Scientific, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 20 devices →

Related Devices (Code: CIG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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